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1.
Mater Sci Eng C Mater Biol Appl ; 80: 594-602, 2017 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-28866206

RESUMEN

Adhesion, proliferation and differentiation of dental pulp stem cells (DPSCs) into chondrocytes were investigated in this work with the purpose of broadening the array of cell alternatives to the therapy of cartilage lesions related to tissue engineering approaches. A porous chitosan-xanthan (C-X) matrix was used as scaffold and kartogenin was used as a selective chondrogenic differentiation promoter. The scaffold was characterized regarding aspect and surface morphology, absorption and stability in culture medium, thickness, porosity, thermogravimetric behavior, X-ray diffraction, mechanical properties and indirect cytocompatibility. The behavior of DPSCs cultured on the scaffold was evaluated by scanning electron microscopy and cell differentiation, by histological analysis. A sufficiently stable amorphous scaffold with mean thickness of 0.89±0.01mm and high culture medium absorption capacity (13.20±1.88g/g) was obtained, and kartogenin concentrations as low as 100nmol/L were sufficient to efficiently induce DPSCs differentiation into chondrocytes, showing that the strategy proposed may be a straightforward and effective approach for tissue engineering aiming at the therapy of cartilage lesions.


Asunto(s)
Pulpa Dental , Anilidas , Diferenciación Celular , Proliferación Celular , Células Cultivadas , Quitosano , Condrocitos , Humanos , Ácidos Ftálicos , Polisacáridos Bacterianos , Porosidad , Células Madre , Ingeniería de Tejidos , Andamios del Tejido
2.
BMC Geriatr ; 14: 13, 2014 Jan 31.
Artículo en Inglés | MEDLINE | ID: mdl-24484283

RESUMEN

BACKGROUND: The purpose of this study was to investigate the influence of muscle mass and bone mineral density on markers of mobility in dwelling elderly women. METHODS: This cross-sectional study included 99 elderly women, who were 65 years old or above, in Campinas-SP, Brazil. To collect data, we used sociodemographic data, the body mass index (BMI), health status, comorbidities, use of medications, mobility tests (TUG and gait speed) and examinations of the body composition (densitometry with dual-emission X-ray absorptiometry "DXA"). In order to examine the relationship between muscle and bone mass with mobility (gait speed and TUG), we applied the Spearman correlation coefficient.Also was applied the analysis of covariance (ANCOVA) adjusted for age and comorbidities. To identify the factors associated with mobility, we used the univariate and multivariate logistic regression analysis. The level of significance for statistical tests was P < 0.05. RESULTS: The correlation between sarcopenia and bone mineral density with mobility tests showed a significant relationship only between sarcopenia and TUG (r = 0.277, P = 0.006) in Spearman correlation coefficient. The result of the correlation analysis (ANCOVA) showed that sarcopenia was associated with gait speed (r2 = 0.0636, P = 0.0018) and TUG (r2 = 0.0898, P = 0.0027). The results of the multivariate analysis showed that age (P = 0.034, OR = 1.081) was associated with worse performance on gait speed. By highlighting the TUG test, the results of the multivariate analysis showed that the age (P = 0.004, OR = 1.111) and BMI in overweight (P = 0.011, OR = 7.83) and obese (P < 0.001, OR = 7.84) women were associated with lower performance of the functionality of the lower limbs. CONCLUSION: The findings with regard to mobility tests which were analyzed in this study indicate the association of variables related to the aging process that contribute to the decline in physical performance, for example, age, BMI and sarcopenia.


Asunto(s)
Composición Corporal/fisiología , Densidad Ósea/fisiología , Evaluación Geriátrica/métodos , Limitación de la Movilidad , Fuerza Muscular/fisiología , Anciano , Anciano de 80 o más Años , Estudios Transversales , Femenino , Marcha/fisiología , Humanos , Músculo Esquelético/fisiología
3.
Geriatr Gerontol Int ; 13(4): 1043-50, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23506046

RESUMEN

AIM: In the elderly population, rheumatic conditions are major causes of pain that restrict participation in activities and mobility, and cause difficulties in the execution of self-care tasks. The present study aimed to analyze the prevalence and factors associated with the self-reported rheumatic diseases and chronic joint symptoms of the elderly. METHODS: This transversal epidemiological survey involved 2209 older adults (aged ≥ 60 years). The investigation included sociodemographic factors, anthropometrics, activities of daily living, chronic conditions, medication and quality of life. Univariate and multivariate regression analysis were used for statistical procedures, P ≤ 0.05. RESULTS: The prevalence of rheumatism was 22.7%. Multivariate analysis showed that rheumatism was correlated with the following: female sex (OR = 1.91), high income (OR = 2.34), cardiovascular disease (OR = 1.42), cataracts (OR = 1.39), glucocorticoids (OR = 5.24), other anti-inflammatory medications (OR = 2.24) and pain (OR = 0.983). After adjusting for age and glucocorticoids, an association between cataracts and rheumatism was detected (OR = 1.32). The prevalence of symptoms was 45.6%. Multivariate regression results for symptoms included the following: female sex (OR = 1.40), body mass index ≥ 30.0 kg/m(2) (OR = 3.31), functional capacity (OR = 0.990), general health (OR = 0.993) and pain (OR = 0.981). After adjustment for age and glucocorticoids, an association between cataracts and symptoms was detected (OR = 1.26). CONCLUSION: There was a significant association of rheumatism and symptoms with women and high incomes. Obesity was associated with joint symptoms, which in turn were associated with an impaired quality of life. Cataracts and cardiovascular disease were associated with rheumatism. The identification of these characteristics in the elderly will contribute to a better understanding of this systemic disease and should be used to plan effective preventive measures.


Asunto(s)
Artropatías/epidemiología , Enfermedades Reumáticas/epidemiología , Anciano , Enfermedad Crónica , Estudios Transversales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Prevalencia , Factores de Riesgo
4.
J Rheumatol ; 37(7): 1519-26, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20472924

RESUMEN

OBJECTIVE: Mature articular cartilage is vulnerable to injuries and disease processes that cause irreversible tissue damage because of its limited capacity for self-repair. Umbilical cord blood is a source of mesenchymal stem cells, which can give rise to cells of different lineages, including cartilage, bone, and fat. Cellular condensation is a required step in the initiation of mesenchymal chondrogenesis. We attempted to differentiate cells from umbilical cord blood into chondrocytes with insulin-like growth factor 1 (IGF-1) and transforming growth factor-ss3 (TGF-ss3). METHODS: Cells were grown in high density micromass and monolayer culture systems and then evaluated for expression of type II collagen, aggrecan, and Sox9. Umbilical cord blood from 130 patients was harvested. RESULTS: Expression of type II collagen, aggrecan, and Sox9 was detected after 14 days in TGF-ss3- and IGF-1-stimulated cells in both types of culture (monolayer and micromass). On Day 21 in the micromass culture, expression levels were greater than they were at 14 days for all genes. TGF-ss3 was found to be more efficient at promoting chondrogenesis than IGF-1. By western blot, we also found that after 3 weeks, the expression of type II collagen was greater in micromass culture with TGF-ss3. CONCLUSION: TGF-ss3 used in micromass culture is the best growth factor for promoting the proliferation and differentiation of mesenchymal cells from umbilical cord blood during chondrogenesis. This approach may provide an alternative to autologous grafting.


Asunto(s)
Diferenciación Celular/efectos de los fármacos , Condrogénesis/efectos de los fármacos , Sangre Fetal/citología , Factor I del Crecimiento Similar a la Insulina/farmacología , Células Madre Mesenquimatosas/efectos de los fármacos , Células Madre Mesenquimatosas/fisiología , Factor de Crecimiento Transformador beta3/farmacología , Agrecanos/genética , Agrecanos/metabolismo , Células Cultivadas , Condrogénesis/fisiología , Colágeno Tipo II/genética , Colágeno Tipo II/metabolismo , Humanos , Células Madre Mesenquimatosas/citología , Factor de Transcripción SOX9/genética , Factor de Transcripción SOX9/metabolismo
5.
Rheumatol Int ; 30(12): 1669-72, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19789875

RESUMEN

A 43-year-old woman reported pain in the right hypochondrium, which had started 3 years before and had been worsening for the past few days. Claudication in the superior and inferior limbs, diffuse myalgia, dyspnea, precordialgia followed by dizziness and visual turbidity were added to the clinical picture. In the physical examination bilateral carotid bruit was observed, abdominal aorta murmur and the decrease of the right radial and left pedis pulses and arterial hypertension with difference in the diastolic pressure between limbs >10 mmHg was also observed. On cardiac catheterisation with aortography, right coronary with proximal parietal irregularities, slight pressure increase in right chambers and pulmonary artery, preserved left ventricle contractility, competent valves, carotid and subclavian partial obstruction, severe narrowing of the abdominal aorta below the diaphragm (80%) and right renal artery significant stenosis were observed. Takayasu's arteritis (TA) diagnosis was established according to the ACR criteria based on the clinical symptomatology, on physical and image test findings. Two years later she presented malar rash, photosensitivity, nephropathy, leukopenia, lymphopenia and hemolytic anemia confirming the systemic lupus erythematosus (SLE) diagnosis. TA coexisting with SLE has rarely been reported.


Asunto(s)
Lupus Eritematoso Sistémico/complicaciones , Arteritis de Takayasu/complicaciones , Adulto , Amiodarona/uso terapéutico , Femenino , Humanos , Lupus Eritematoso Sistémico/tratamiento farmacológico , Lupus Eritematoso Sistémico/patología , Nifedipino/uso terapéutico , Prednisona/uso terapéutico , Arteritis de Takayasu/diagnóstico , Arteritis de Takayasu/tratamiento farmacológico , Resultado del Tratamiento
7.
J Rheumatol ; 30(12): 2632-7, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14719206

RESUMEN

OBJECTIVE: To analyze the profile of the HLA-B27 and B7 cross-reactive group (CREG) alleles and the role of these markers in disease characterization and progression in patients with undifferentiated spondyloarthropathies (uSpA). METHODS: A total of 80 patients with a diagnosis of uSpA (40 HLA-B27 positive and 40 HLA-B27 negative) were prospectively studied for 2 years. The control group consisted of 66 HLA-B27 positive and 112 HLA-B27 negative individuals without a history of seronegative SpA. HLA-B alleles were typed at low (B7-CREG alleles, i.e., B*7, B*54, B*55, B*56, B*40, B*42) or high resolution (B*27 alleles) using polymerase chain reaction-amplified DNA hybridized with sequence-specific oligonucleotide probes. RESULTS: HLA-B*2705 was the most frequent allele, observed in 92.5% of the patients and in 77% of the controls, followed by the HLA-B*2702, observed in 5% of the patients and in 12% of the controls. HLA-B*2704 was observed in only one patient (2.5%), and was absent in the control population. HLA-B*2703 (6%) and HLA-B*2707 (5%) alleles were observed only in controls. No associations between HLA-B*27 alleles or B7-CREG alleles and any specific manifestation of uSpA were observed. HLA-B27 positive patients more frequently presented juvenile onset SpA (p = 0.002) and progression to ankylosing spondylitis (AS) (p = 0.03) than did HLA-B27 negative patients. The B7-CREG alleles were observed in 5% of the HLA-B27 positive uSpA group, in 25% of the HLA-B27 negative uSpA group, in 7% of the HLA-B27 positive controls, and in 13% of the HLA-B27 negative controls; a significant association was observed between the presence of the B7-CREG and the HLA-B27 negative uSpA group (p = 0.012). CONCLUSION: The frequency of the HLA-B*2705 allele among the B27 positive uSpA patients of this series was closely similar to that reported for patients with ankylosing spondylitis (AS). The presence of HLA-B*27 alleles was associated with the progression to AS, and the presence of B7-CREG was associated with uSpA in the HLA-B27 negative group.


Asunto(s)
Alelos , Predisposición Genética a la Enfermedad , Antígeno HLA-B27/genética , Antígeno HLA-B7/genética , Espondilitis/genética , Adolescente , Brasil/epidemiología , Niño , Progresión de la Enfermedad , Femenino , Humanos , Lactante , Articulaciones/patología , Masculino , Pacientes Ambulatorios , Estudios Prospectivos , Espondilitis/epidemiología , Espondilitis/patología
8.
Rev. bras. reumatol ; Rev. bras. reumatol;40(4): 175-182, jul.-ago. 2000. tab
Artículo en Portugués | LILACS | ID: lil-308805

RESUMEN

Objetivos: Avaliar a densidade mineral óssea (DMO) em pacientes com lúpus eritematoso sistêmico (LES), determinar o papel dos corticosteróides e drogas citostáticas, e analisar os efeitos dos estrogênios sobre a densidade mineral óssea no LES. Pacientes e Métodos: Avaliou-se a DMO vertebral (L2-L4) e do fêmur proximal em 60 pacientes com LES na pós-menopausa e em 64 controles. Também os níveis de estradiol plasmático foram medidos. A idade, idade ao início da doença, índice de massa corpórea (IMC), tempo de doença, atividade de doença (pelo SLEDAI), doses de prednisona no momento da avaliação, cumulativa do último ano e cumulativa total, bem como o uso de drogas citostáticas, também foram analisados. Resultados: A média dos níveis de estradiol entre as pacientes foi de 175,8 pg/ml e, entre as mulheres do grupo controle, 149,9. A DMO foi significativamente menor nas pacientes do que nas mulheres sadias (P<0,0001). As médias de doses atual, cumulativa total e do último ano foram, respectivamente, de 19,17 mg/dl, 28,78g e 5,33g. Não houve associação entre as doses de corticosteróides ou de outras drogas citostáticas utilizadas e a perda de massa óssea. As concentrações séricas de estradiol não influíram na perda de massa óssea. O IMC e a idade da paciente ao início da doença, conjuntamente, influíram sobre a DMO em vértebra L2. Conclusão: A DMO foi significativamente menor entre as pacientes com LES sem associação com as doses de corticosteróides ou outras drogas utilizadas. Os níveis de estradiol não parecem influir sobre a DMO nessas pacientes. Baixo IMC interagindo com baixa idade da paciente ao início da doença parece influir sobre a probabilidade de perda de massa óssea no LES


Asunto(s)
Humanos , Femenino , Adolescente , Adulto , Persona de Mediana Edad , Densidad Ósea/fisiología , Estrógenos , Lupus Eritematoso Sistémico/fisiopatología , Corticoesteroides
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